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European Journal of Medical Genetics|December 14, 2018
Rare missense TUBGCP5 gene variant in a patient with primary microcephalyAleš Maver, Goran Čuturilo, Anja Kovanda, et al.
Plos One|September 26, 2013
Expression signature as a biomarker for prenatal diagnosis of trisomy 21Marija Volk, Aleš Maver, Luca Lovrečić, et al.
Gene|February 15, 2019
MiRNA as biomarker for uveitis - A systematic review of the literatureSasa Pockar, Mojca Globocnik Petrovic, Borut Peterlin, et al.
Orphanet Journal of Rare Diseases|February 28, 2025
TTN:c.12478del in proximal I-band of titin represents a common molecular cause of dilated cardiomyopathy in Slovenian patientsNina Vodnjov, Andraž Cerar, Aleš Maver, et al.
Molecular Genetics & Genomic Medicine|April 21, 2019
The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancyGorazd Rudolf, Luca Lovrečić, Nataša Tul, et al.
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG|October 1, 2015
Common chitotriosidase duplication gene polymorphism and clinical outcome status in sarcoidosisMatevž Harlander, Aleš Maver, Marjeta Terčelj, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|September 24, 2017
A Single Nucleotide Polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortionAnita Barišić, Nina Pereza, Alenka Hodžić, et al.
Omics : a Journal of Integrative Biology|October 20, 2017
Transcriptome Profiling Uncovers Potential Common Mechanisms in Fetal Trisomies 18 and 21Marija Volk, Aleš Maver, Alenka Hodžić, et al.
Genetics and Molecular Biology|May 17, 2018
Genetic variations in circadian rhythm genes and susceptibility for myocardial infarctionIvana Škrlec, Jakov Milic, Marija Heffer, et al.
Reproductive Biomedicine Online|March 13, 2012
Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortionNina Pereza, Saša Ostojić, Marija Volk, et al.
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